Etchant and method of use

ABSTRACT

A method of anisotropically etching a semiconductive substrate uses a hydrofluorocarbon etch gas with an etch selectivity fluorocarbon gas. The fluorocarbon gas is used under conditions that enhance selectivity of the etch to an etch stop layer with respect to a bulk dielectric material such as doped or undoped silicon dioxide. In one method, a silicon dioxide dielectric layer is provided upon an etch stop layer, wherein the etch stop layer comprises silicon dioxide that is doped differently from the silicon dioxide dielectric layer. A gaseous etchant including a hydrofluorocarbon etch gas and a fluorocarbon selectivity compound is provided, and the silicon dioxide dielectric layer is exposed to the gaseous etchant.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 10/888,255, filed Jul. 9, 2004, pending, which application is a divisional of U.S. patent application Ser. No. 09/559,504, filed on Apr. 27, 2000, now U.S. Pat. No. 6,890,863, issued May 10, 2005, the disclosures of which are incorporated herein by reference.

BACKGROUND OF THE INVENTION

1. The Field of the Invention

The present invention relates to semiconductor device fabrication. More particularly, the present invention relates to etch processing of semiconductor structures. In particular, the present invention relates to a contact hole etch and process therefore that operates in the subhalf-micron range, where the etchant includes a compound that is used as a selectivity enhancer.

2. State of the Art

In the microelectronics industry, a “substrate” refers to one or more semiconductor layers or structures which includes active or operable portions of semiconductor devices. In the context of this document, the term “semiconductive substrate” is defined to mean any construction comprising semiconductive material including, but not limited to, bulk semiconductive material such as a semiconductive substrate, either alone or in assemblies comprising other materials thereon, and semiconductive material layers, either alone or in assemblies comprising other materials. The term “substrate” refers to any supporting structure including, but not limited to, the semiconductive substrates described above.

Miniaturization is the process of crowding an ever-increasing number of microelectronic devices into the same amount of semiconductive substrate real estate while maintaining and/or improving the quality of each microelectronic device. Miniaturization also requires improving and/or maintaining the integrity of interconnects and vias. The pressure to fabricate ever-smaller microelectronic devices on the active surface of semiconductive substrates consequently requires the formation of smaller topographical features that define the components of the microelectronic devices. One feature is the contact corridor, also known as the contact hole or channel (hereinafter “contact”) which typically comprises a circular depression that extends through a dielectric layer to an underlying structure that is electrically conductive or electrically semiconductive.

As the miniaturization process progresses into the subhalf-micron range, structural dimension tolerances become increasingly important such that processing sensitivity must be correspondingly improved. As an example, a contact in the subhalf-micron range preferably retains a critical dimension (CD) within a defined tolerance during a high-aspect ratio anisotropic etch through a dielectric layer. The contact, therefore, must retain its initial circular cross section and constant diameter cylindrical shape within the dielectric layer in order to avoid cutting into an underlying structure outside of the CD. Additionally, the CD cannot become so small that an open circuit is created due to the inability to fill the contact, or a destructively high resistance created by too narrow of a contact.

As used herein, the term “high-aspect ratio” refers to depth-to-bottom CD ratio of about five to one or more. In addition to contacts, high-aspect ratio subhalf-micron width lines or trenches within a dielectric layer must be fabricated under conditions that require similar etch tolerances.

A dry, or plasma etch in an etch tool is the preferred process for etching a subhalf-micron contact. Inductively coupled, or high density etch systems are commonly referred to as etch tools. It would be desirable to etch a high-aspect ratio contact through a layer of dielectric in an etch tool while retaining the preferred CD.

Dielectrics may be materials such as borophosphosilicate glass (BPSG) or other materials such as oxides, nitrides, or dielectric anti-reflective coatings (DARC) that are placed between the mask and the substrate silicon. Processing parameters for the etching of a contact require the ability to maintain a CD for about a 2.2 microns deep feature, overetched by 0.4 microns and to generate a contact profile that is preferably only slightly tapered or more preferably substantially cylindrical. At the subhalf-micron geometry, an increase in the radius of the contact caused by a re-entrant profile may be sustained up to about 0.025 microns. Contacts with a depth of about 2.2 microns and between 0.2 and 0.45 microns for a CD would be considered to have achieved the required CD profile control.

Because the etching process typically involves a silicon oxide such as BPSG and an etch stop layer such as silicon nitride or other materials including doped or undoped silicon oxide, enhanced selectivity to the etch stop layer is required as fabrication proceeds into the subhalf-micron regime.

Another problem that exists in the prior art is that different etch types require different chamber wall temperatures. Where a high chamber wall temperature etch must be followed by a lower chamber wall temperature etch, transfer of the semiconductive substrate from the high chamber wall temperature etch to a low chamber wall temperature etch is required because of the inability to cool the high-temperature etch chamber rapidly enough. Attempting to conduct a lower temperature etch in a hot, high-temperature etch chamber may cause the lower temperature etch to malfunction and to consequently damage or destroy the semiconductor device being fabricated. It is therefore necessary to transfer the semiconductive substrate out of the high-temperature etch chamber into a lower temperature etch chamber. Such a transfer is both time consuming and technically difficult where the necessity of maintaining the clean environment requires a transfer to an etch chamber that may be remote and thermally insulated from the high-temperature etch chamber. It would therefore be an improvement in the art to discover a method of etching for two traditionally different temperature etches with a closer temperature range or the same temperature range.

Applied Materials, Inc. of Santa Clara, Calif. currently offers an inductively-coupled plasma etcher identified as the Dielectric Etch IPS Centura® system (the “IPS system”) for etching high-aspect ratio contacts, among other uses. The IPS system uses an inductively-coupled, parallel plate technology that employs temperature controlled Si surfaces within the etch chamber in combination with fluorine-substituted hydrocarbon etch gases to achieve an oxide etch having a selectivity to silicon nitride in excess of ten to one. U.S. Pat. No. 5,423,945, assigned to Applied Materials, Inc., discloses the structure of operation of a predecessor apparatus to the IPS system, a schematic of which is shown in FIG. 1. The disclosure thereof is incorporated herein by specific reference.

An IPS system 10 as depicted in FIG. 1 includes an etch chamber 12 primarily defined between a grounded silicon roof 14, an RF powered (bias) semiconductive substrate support 16 and a silicon ring 18 surrounding semiconductive substrate support 16, on which a semiconductive substrate 100 is disposed for processing. A plasma 20 generated over semiconductive substrate 100 is confined by magnetic fields as seen at reference numerals 22 and 24. Gases are supplied to chamber 12 through a valved manifold 26 which is connected to a plurality of gas sources (not shown). Evacuation of etch chamber 12 may be effected as desired through a valve 28, as is known in the art.

An RF source power is supplied to an inner antenna 30 and an outer antenna 32 by an RF generator 34. The inner and outer antennae 30 and 32 are tuned for resonance in order to provide an efficient inductive coupling with plasma 20. Inner antenna 30, outer antenna 32, RF generator 34 and associated circuitry comprise a source network 36. Bias power is also supplied to semiconductive substrate support 16 by RF generator 34. RF generator 34, supplying power to semiconductive substrate support 16, comprises a bias network 38 with associated circuitry as shown. RF bias power is delivered at 1.7±0.2 MHz, RF outer antenna power at 2.0±0.1 MHz, and RF inner antenna power at 2.3±0.1 MHz. Other details of IPS system 10 being entirely conventional, no further discussion thereof is required. Semiconductive substrate 100 is attached to a monopolar electrostatic chuck as a semiconductive substrate support 16.

A plasma etch process that was initially developed for use with the IPS system employs a gas flow of a relatively high rate and somewhat complex chemistry, relatively high process temperatures and, most notably, CO (carbon monoxide) in the gas mixture. Specifically, the process employs 300-400 (and preferably 358) standard cubic centimeters per minute (sccm) Ar (argon), 55 sccm CO, 82 sccm CHF₃ (trifluoromethane), and 26 sccm CH₂F₂ (difluoromethane) with a process pressure of 50 mTorr. Source power input is about 1650 watts, apportioned as 1400 watts to the outer antenna and 250 watts to the inner antenna. Bias power is about 800 watts. According to the IPS system manufacturer, the high volume of Ar is required, or at least desirable, to maintain a plasma state within the etch chamber.

The IPS system employs the adjustable, dual-antenna inductive source and bias power control to adjust etch results. All high density oxide etch tools such as the IPS system can deposit from about 2,000 to about 4,000 angstroms per minute of fluorocarbon polymers on the semiconductive substrate under conditions if the bias power is set to zero. In other words, any surface that is not powered is exposed to a flux of pre-polymer material that will deposit on the surface unless conditions are altered to prevent its deposition.

Capacitative coupling is often a source of difficulty during etching. The common assignee of the present invention has filed several patent applications regarding the control of this capacitative coupling, including U.S. application Ser. No. 09/012,155, now U.S. Pat. No. 6,095,159, entitled “Method of Modifying an RF Circuit of a Plasma Chamber to Increase Chamber Life and Process Capabilities”; U.S. application Ser. No. 09/031,400, now U.S. Pat. No. 6,516,742, entitled “Apparatus for Improved Low Pressure Inductively Coupled High Density Plasma Reactor”; and U.S. application Ser. No. 09/020,696, now U.S. Pat. No. 5,998,931, entitled “Method and Apparatus for Controlling Electrostatic Coupling to Plasmas.” The disclosures of the aforementioned three patents are incorporated herein by reference.

Some of the high density oxide etch tools have virtually no capacitative coupling between the source coil and the plasma. For example, the IPS system, as identified hereinabove has virtually no such coupling. The conducting silicon roof on the IPS system acts as an electrostatic shield which eliminates electrostatic coupling between the source coil and the plasma. Thus, roof temperature may be used to control the amount of deposition that occurs on the roof of the IPS system. Additionally, the IPS system uses a reactive surface to line the chamber walls or parts of the walls. The IPS system uses silicon which it heats to temperatures that are too high to permit deposition but that are sufficiently high to scavenge free fluorine from the etch plasma.

It would be advantageous to develop a process for use with the IPS system or an equivalent system that would be simple and easy to control and optimize while still meeting manufacturing specifications for the high-aspect ratio contacts and other apertures, such as lines or trenches which may be formed in a substrate. Such a process would be expected to yield similar results in any inductively-coupled plasma etcher which employs silicon surfaces at elevated temperatures within the etch chamber.

It would also be advantageous to develop a process for use with the IPS system which would be versatile enough to allow different etch types to be conducted on the same semiconductive substrate without requiring a transfer of the semiconductive substrate from one etch tool to another due to disparate temperature differences between the two etch types.

SUMMARY OF THE INVENTION

The present invention relates to a process for anisotropically etching through silicon dioxide and stopping on an underlying layer. The present invention provides a process that is suitable for use in a high density etch tool, such as the Applied Materials IPS Centura® system, for etching silicon dioxide by employing an inventive gas mixture and delivering the gas mixture at a low flow rate and at relatively low process temperatures. Under these conditions, the low temperatures used in the inventive method allow the use of an etch gas mixture that etches the silicon dioxide dielectric layer substantially anisotropically and which stops etching on an underlying layer that is compositionally dissimilar to the silicon dioxide dielectric layer. The underlying layer can be composed of a nitride compound such as a refractory metal nitride or silicon nitride, or it may be a silicon dioxide underlying layer with different doping from the silicon dioxide dielectric layer. Alternatively, the underlying layer may be a silicon material such as a monocrystalline silicon substrate or it may be polysilicon.

The inventive process employs a mixture of two preferred etchant gases: a hydrofluorocarbon and a selectivity compound consisting of carbon and fluorine, wherein the latter is a selectivity enhancing gas that is preferably one of CF₄, C₂F₆, C₄F₈, C₅F₆, C₅F₈, and combinations of these. The etch gas flow rates are extremely low. The etch gas flow rates are on the order of about 30 to about 50 sccm of hydrofluorocarbon, preferably CHF₃. The selectivity enhancing gas flow rate is from about zero to about 25 sccm of the selectivity compound, preferably CF₄.

Etch selectivity fluorocarbon gases, intended herein to mean CF₄, C₂F₆, C₄F₈, C₅F₆, C₅F₈, and the like and combinations of these, have been used in previous applications as etch gases, but not as a selectivity enhancing etch gas for nitride or silicon compounds while etching oxides on semiconductive substrates. During development of the present invention, it was discovered that under the operating conditions set forth herein, increased etch selectivity fluorocarbon etch gas in addition to the hydrofluorocarbon etch gas such as CHF₃ etch gas, caused an increased etch selectivity for a nitride compound, or a silicon dioxide underlying layer doped differently from the silicon dioxide dielectric layer.

The present invention is also useful for processing different types of etches such as a mask-aligned contact etch at an etch chamber roof surface temperature in a range below about 200° C. and a self-aligned contact etch in the same etch chamber in the same temperature range. Thereby, etching may be carried out within the same etch chamber where previously self-aligned contact etching needed to be carried out in a high-temperature etch chamber, or the high-aspect ratio mask-aligned contact etch chamber could be used but a significant amount of time was needed to allow the etch chamber to cool.

These and other features of the present invention will become more fully apparent from the following description and appended claims, or may be learned by the practice of the invention as set forth hereinafter.

BRIEF DESCRIPTION OF THE DRAWINGS

In order to illustrate the manner in which the above-recited and other advantages and features of the invention are obtained, a more particular description of the invention briefly described above will be rendered by reference to specific embodiments thereof which are illustrated in the appended drawings. Understanding that these drawings depict only typical embodiments of the invention and are not therefore to be considered limiting of its scope, the invention will be described and explained with additional specificity and detail through the use of the accompanying drawings in which:

FIG. 1 is a cross-sectional and wiring schematic of the Applied Materials, Incorporated Dielectric Etch IPS Centura® system, suitable for use with the process of the present invention and together therewith comprising an embodiment of an inventive etch system;

FIG. 2A is an elevational cross-sectional view of a semiconductive substrate that has been patterned with a mask in preparation for a self-aligned contact etch;

FIG. 2B is an elevational cross-sectional view of the semiconductive substrate depicted in FIG. 2A, taken along the line B-B;

FIG. 3 is an elevational cross-sectional view of the semiconductive substrate seen in FIG. 2A under etch conditions disclosed herein without the presence of CF₄;

FIG. 4 is an elevational cross-sectional view of the semiconductive substrate seen in FIG. 2A under etch conditions containing about a 10% gas presence of CF₄;

FIG. 5 is an elevational cross-sectional view of the semiconductive substrate depicted in FIG. 2A under etch conditions containing about a 25% gas presence of CF₄; and

FIG. 6 is an elevational cross-sectional view of a semiconductive substrate with a high-aspect ratio contact formed therein.

DETAILED DESCRIPTION OF THE INVENTION

The present invention employs two etchant gases: a hydrofluorocarbon etch gas and an etch selectivity fluorocarbon gas. The gas flow rates are extremely low, on the order of from about 30 to about 50 sccm (standard cubic centimeters per minute) for the hydrofluorocarbon gas and from about zero to about 25 sccm for the etch selectivity fluorocarbon gases. The hydrofluorocarbon etch gas may include CHF₃, CH₂F₂, CH₃F, C₂HF₅ and the like, and combinations of these. The etch selectivity fluorocarbon gases may include CF₄ or quantities of the higher carbon fluorocarbons such as C₂F₆, C₄F₈, C₅F₆, C₅F₈, and the like and combinations of these. The etch selectivity fluorocarbon gases provide enhanced selectivity under the inventive process conditions instead of their usual behavior as selectivity reducers.

Under relatively low pressure processes in the range from about 10 to about 40 mTorr, the above-mentioned flow rates are preferred. For higher pressure processes in the range of from about 40 to about 100 mTorr, higher proportional flow rates may be used. For example, CHF₃ and CF₄ flows may be in the range from about 60 to about 100 sccm.

The inventive etch method is carried out in dielectric materials, by way of example in the form of boron phosphorus silicate glass (BPSG) and other doped and undoped dielectric films used in semiconductive microelectronic device fabrication. Such doped and undoped dielectric films may include SiO₂, tetraethyl orthosilicate (TEOS), and phosphorous silicate glass (PSG).

A variant of the inventive process employs only a hydrofluorocarbon such as CHF₃ during the initial portion of the etch process and adds an etch selectivity fluorocarbon gas in the final portion of the etch process to increase the etch selectivity to the underlying layer such as a silicon nitride layer (Si₃N₄ and the like) or other compositionally dissimilar dielectric layers, such as a silicon dioxide underlying layer with different doping from the silicon dioxide dielectric layer.

Another variant of the inventive process employs the injection of a hydrofluorocarbon gas such as CHF₃ during the etch process and pulses an etch selectivity hydrofluorocarbon gas such as CF₄ over a concentration range and for a pulse time period to improve the etch selectivity to the underlying layer.

Reference will now be made to the figures wherein like structures will be provided with like reference designations. It is to be understood that the drawings are diagrammatic and schematic representations of some embodiments of the present invention and are not limiting of the present invention nor are they necessarily drawn to scale.

The system chamber, referring to FIG. 1, is defined and controlled at roof 14 over semiconductive substrate end ring 18 surrounding semiconductive substrate 100. Roof 14 also has sidewalls as depicted and is held to a roof surface temperature within a range from about 100° C. to about 190° C., more preferably from about 100° C. to less than about 150° C., and most preferably from about 100° C. to less than about 140° C. Ring 18 is held within a range from about 180° C. to about 300° C., preferably from about 190° C. to about 250° C., and most preferably about 200° C. A preferred temperature comprises the lowest at which the IPS system is operable under continuous semiconductive substrate processing conditions. Further, a roof temperature below about 140° C. is the preferred temperature which may be employed with the inventive gas mixture to conduct the selective etch process of the invention without experiencing over-etching of the silicon nitride or silicon structures which are present in a microelectronic device beneath a compositionally different bulk dielectric. A roof temperature of about 200° C. is also acceptable.

The temperature of semiconductive substrate support 16 is contained in a range from between about −20° C. to about +80° C. and most preferably about +40° C. The pressure of etch chamber 12 is maintained at greater than about 1 mTorr, more preferably greater than about 15 mTorr, and most preferably greater than about 20 mTorr.

Source power to etch chamber 12 is preferably maintained between about 750 and about 1250 Watts, at a ratio of about four to one between outer antenna 32 and inner antenna 30, and most preferably about 1000 Watts with about 875 Watts to outer antenna 32 and about 125 watts to inner antenna 30. Bias power at semiconductive substrate support 16 is preferably maintained at about 400 to about 800 Watts, preferably from about 500 to about 700 Watts, and most preferably about 600 Watts.

The process parameters disclosed herein have been used to produce high-aspect ratio CD features. The CD features were defined through BPSG using an I-line photoresist as well as deep ultraviolet (DUV) photoresist. Specifically, the CD features formed using I-line photoresist where in a range from about 0.2 microns to about 0.6 microns, and from about 0.2 microns to about 0.4 microns. For a DUV photoresist, the CD features formed greater than or equal to about 0.1 microns to about 0.5 microns, from about 0.2 microns to about 0.4 microns, and about 0.3 microns. A suitable example of an I-line resist is the Sumitomo PFI-66A7 resist, offered by Sumitomo of Osaka, Japan while a suitable DUV resist is the TOK-TOUR-P024 resist, offered by TOK of Sagami, Japan.

Two-Stage Gas Etching

A first embodiment of the present invention includes providing a semiconductive substrate 100 in an etch tool such as the Applied Materials IPS system. Referring to FIG. 2A, etching is carried out by patterning a mask 40 upon a bulk dielectric 42 that is disposed about spacers 44. Spacers 44 may cover structures such as a gate stack 46. Gate stack 46 is disposed upon a gate oxide layer 48 that is ultimately disposed upon a semiconductive material 50.

Dielectric 42 is composed of silicon dioxide (SiO₂) which can be described as being either undoped or doped glass. In the semiconductor industry, the term oxide is generally used instead of glass. Generally, an undoped oxide is either a field oxide or gate oxide which is usually grown in a furnace. Doped oxides include BPSG, PSG, etc. which are generally formed on silicon semiconductive substrate 100 with a dopant gas(es) during a deposition process. Dielectric 42 is deposited onto adjacent, spaced apart gate stacks 46 as well as other surfaces on semiconductive substrate 100. Gate stacks 46 include spacers 44 and are fabricated by a spacer etch process from an etch stop layer composed of silicon nitride or a silicon oxide material that is compositionally different from dielectric 42.

Mask 40 comprises a photoresist layer having an opening 56 for forming a predetermined pattern. Typically, this is accomplished using a semiconductor photomask and known conventional etch mask patterning techniques.

FIG. 2B is an elevational cross-sectional view of semiconductive substrate 100 depicted in FIG. 2A, taken along the section line B-B to depict a perpendicular view thereof. The etch is also useful for stopping on structures such as a shallow trench isolation 60 as depicted in FIG. 2B. An etch profile 62 is contemplated with the present invention that may cause a slight taper shape as the contact is formed beginning at opening 56. Additionally, the etch will stop at and/or pass beyond spacers 44, depicted in FIG. 2B as a phantom line as spacers 44 are not intersected by section line B-B.

The gas plasma etch technique employed herein typically has an etching area in a plasma and is generated under vacuum within the confines of an RF discharge unit. The preferred plasma etch technique employed herein may include the use of Electron Cyclotron Resonance (ECR), reactive ion etch (RIE), magnetically enhanced reactive ion etch (MERIE), Plasma etching (PE) reactive ion, point plasma etching, magnetically confined helicon and helical resonator, PE, or magnetron PE. In plasma dry etchers, typically the upper electrode is powered while the lower electrode is grounded. In RIE etching, the lower electrode is powered while the upper electrode is grounded. In triode dry etchers, the upper and lower electrodes can be powered as well as the sidewall. In MERIE etching, magnets are used to increase the ion density of the plasma. In ECR etching, the plasma is generated upstream from the main reaction chamber. This produces a low ion energy to reduce damage to the semiconductive substrate.

A semiconductor device is located in a desired etcher within an etching area and is etched with a fluorinated chemical etchant system to form a predetermined pattern therein. The fluorinated chemical etchant system may comprise a chemical etchant composition of the type described above such as CHF₃, CF₄, Ar, and optionally a CH₂F₂ additive material. The fluorinated chemical etchant system is substantially in a gas phase during the etching of the multilayer structure.

Referring again to FIG. 2A, the exposed dielectric 42, composed of SiO₂, is etched anisotropically at a relatively high etch rate down to spacers 44, composed of Si₃N₄ or a differently doped SiO₂ compared to dielectric 42, and serving as an etch stop layer. Portions of dielectric 42 are selectively removed by chemically enhanced ionic bombardment. Some areas of semiconductive substrate 100 continue to have the SiO₂ of dielectric 42 available to be etched while other areas of semiconductive substrate 100 are not etched in that the etch has already exposed spacer 44 where the etching process effectively stops because of polymer formation on the surface of spacer 44. In this way, the etching process can provide for the formation of the upright sidewalls in etched layers which are substantially conformal to the remaining surface while providing etch selectively to the etch stop layer.

When RF energy is applied to the chamber, at least to the upper electrode, the gas fed into the chamber via the gas distribution plate is converted to plasma. The plasma contains reactive chemical species which will etch selected unmasked portions of the semiconductive substrate electrostatically clamped to the lower electrode. A throttle valve located between the plasma etching chamber regulates the pressure of the chamber to processing values, generally in the range of about 10-350 mTorr.

IPS system 10 is governed by a programmable computer that is programmed to prompt the machine to evacuate and vent the load locks, transfer semiconductive substrates to and from the cassettes, elevator, and etch chamber, control the delivery of process gas, RF power, and magnetic field to the plasma etching chamber, and maintain the temperature of the semiconductive substrate in the plasma etching chamber, all at appropriate times and in appropriate sequence.

Given the foregoing environment, a multilayer structure, such as a semiconductor substrate, is located within the plasma etching chamber and is etched with a fluorinated chemical etchant system to form a predetermined pattern therein.

In the case of the chemical etchant composition including CHF₃, CF₄ and Ar, the exposed SiO₂ layer may be selectively etched at a relatively high etch rate and high selectivity down to the Si₃N₄ etch stop layer by removing predetermined portions of the SiO₂ layer using chemically enhanced ionic bombardment of the gas phase etchant material.

Etching is carried out by the formation of a self-aligned contact hole through mask 40 and dielectric 42 that uses a first etch gas, namely the hydrofluorocarbon gas CHF₃ in a first etch gas recipe to a first etch depth. The CHF₃ has a first nitride etch selectivity. Etching continues with an etch selectivity fluorocarbon gas that is blended with the CHF₃ to form a second etch gas recipe. The etch selectivity fluorocarbon gas may include any or all of CF₄, C₂F₆, C₄F₈, C₅F₆, C₅F₈, and the like. The etch selectivity fluorocarbon gas is used in etching the oxide layer as a continuation of the CHF₃ first etch gas. The etch selectivity fluorocarbon gas when blended with the CHF₃ first etch gas has a second nitride selectivity that is greater than the first nitride etch selectivity. Under the inventive conditions, the method of etching the semiconductive substrate stops the self-aligned contact hole upon a nitride layer or upon semiconductive material 50.

As one alternative of this embodiment, the hydrofluorocarbon gas CHF₃ as the first etch gas may be used in connection with CH₂F₂ gas. The ratio of CHF₃ to CH₂F₂ may be from about 10:1 to about 1:10, preferably about 1:1, and most preferably about 5:1.

In another alternative of this embodiment, the hydrofluorocarbon gas CHF₃ is used with the fluorocarbon gas C₂F₆ and may be provided in ratios from about 10:1 to about 5:1, preferably about 10:1.

Preferably for this embodiment, the nitride etch selectivity enhancing gas is the etch selectivity fluorocarbon gas. In a preferred embodiment, the etch selectivity fluorocarbon gas is CF₄. In another embodiment the etch selectivity fluorocarbon gas is provided with CF₄ and C₄F₈. The ratio of CF₄ to C₄F₈ may be in a range from about 10:1 to about 1:10, preferably about 1:1 and most preferably about 5:1. The etch selectivity fluorocarbon gas may also be a combination of CF₄ and C₅F₈. Additionally, it may be the combination of CF₄ and C₅F₆. The relative proportions of CF₄ to its other etch selectivity fluorocarbon gas for the above two examples are in a range from about 10:1 to about 1:10, preferably about 1:1, and most preferably about 5:1.

The relative proportions of the hydrofluorocarbon etch gas to the etch selectivity fluorocarbon gas include the etch gas, particularly CHF₃ in a range from about 30 to about 50 parts in comparison with the etch selectivity fluorocarbon gas in a range from about less than one part to about 25 parts. Preferably, the etch selectivity fluorocarbon gas is supplied in about 15 parts and the first etch gas, particularly CHF₃, is applied in about 44 to about 45 parts.

Where the etch selectivity fluorocarbon gas includes higher carbon number gases including at least one of C₂F₆, C₄F₈, C₅F₆, and C₅F₈, the preferred proportion of the etch selectivity fluorocarbon gas is in a range from about 0.5 to about 4 parts, most preferably from about one part to about 2 parts, in comparison with the first etch gas, particularly CHF₃ which will be in a range from about 30 to about 50 parts, and preferably about 44 to about 45 parts.

Pulsed Fluorocarbon Gas Etching

Another embodiment of the present invention includes providing semiconductive substrate 100 in an etch tool such as the Applied Materials IPS system. Referring again to FIG. 2A, etching is carried out by patterning mask 40 upon bulk dielectric 42 that is disposed about spacers 44. Spacers 44 may cover other structures such as gate stack 46. Gate stack 46 is disposed upon gate oxide layer 48 that is ultimately disposed upon semiconductive material 50.

The pulsed fluorocarbon gas etch technique of this embodiment is carried out under conditions similar to the 2-stage gas etching set forth above. A semiconductor device is located in a desired etcher with an etching area and is etched with the inventive fluorinated chemical etchant system to form a predetermined pattern therein. The fluorinated chemical etchant system may comprise a chemical etchant composition of the type described above such as CHF₃, CF₃, Ar, and optionally a CH₂F₂ additive material. The fluorinated chemical etch system is substantially in a gas phase during the etching of the multi-layer structure.

Exposed dielectric 42, composed of SiO₂, is selectively and anisotropically etched at a relatively high etch rate, and the etch rate is moderated by the pulsing of fluorocarbon gas into the etch recipe.

Etching is carried out by formation of a self-aligned contact hole through mask 40 and dielectric 42 that uses a first etch gas, namely the hydrofluorocarbon gas CHF₃ or the like as a constant etch gas source. Etching is carried out further with the pulsing of an etch selectivity fluorocarbon gas that is intermittently blended with the hydrofluorocarbon gas during the etch process. Pulsing of the fluorocarbon gas is carried out in a range from about 0 sccm to about 25 sccm, preferably from about 15 to about 23 sccm, and most preferably from about 18 to about 22 sccm.

The time period of an overall gas pulsing cycle is in a range from about 10 to about 60 seconds, preferably from about 15 to about 30 seconds. The cycle of the fluorocarbon gas pulse has a period in a range from about 1 second to about 30 seconds, preferably from about 10 seconds to about 20 seconds, and most preferably about 15 seconds.

Determination of a Specific Etch Recipe

In another embodiment of the present invention, a method is provided for etching an oxide disposed upon a nitride with etch selectivity to the nitride layer. This inventive method uses the discovery that a fluorocarbon gas is an etch selectivity enhancer under the inventive conditions, and illustrates a method of finding a preferred etchant gas recipe based upon the inventive discovery.

The method of the second embodiment includes providing an oxide disposed upon a nitride layer that is exposed to a first etching process using CHF₃ with an etch selectivity fluorocarbon gas under the inventive conditions in which the etch selectivity fluorocarbon gas makes the first etching process selective to the nitride layer as set forth above. The inventive method continues by incrementally increasing the etch selectivity fluorocarbon gas and initiating a second etching process for the oxide using the CHF₃ and the increased etch selectivity fluorocarbon gas under conditions which the increased etch selectivity fluorocarbon gas makes the second etching process more selective to the nitride layer than the first etching process. The inventive method may optionally continue by repeating incrementally increasing the etch selectivity fluorocarbon gas and etching the oxide with the CHF₃ and the incrementally increased amount of etch selectivity fluorocarbon gas under the inventive conditions. Accordingly, an increased amount of etch selectivity fluorocarbon gas makes the etch more selective to the nitride layer than the second etching process.

As the degree of etch selectivity is noted in this inventive method, one can then choose a preferred amount of etch selectivity fluorocarbon gas in relation to the CHF₃ to achieve a chosen etch selectivity-to-nitride based upon the first etching process, the second etching process, and the optional etching(s) thereafter. Accordingly, etching may then be carried out on a single semiconductive substrate or upon a batch of semiconductive substrates by etching the oxide to stop on the nitride layer under the chosen etch selectivity-to-nitride conditions.

The etch selectivity fluorocarbon gas may include those gases set forth above and in the ratios among themselves and the proportions to the CHF₃ as set forth above. Preferably, the present invention will be carried out under etching conditions where the roof surface temperature is below about 200° C., preferably below about 160° C., more preferably below about 150° C., and most preferably about 140° C.

In a series of tests, a method was provided for etching a dielectric as depicted in FIG. 2A in order to determine a preferred mixture for a preferred etch recipe that is selective to a nitride etch stop layer. The dielectric 42 is patterned with a mask 40. Dielectric 42 is disposed upon semiconductive material 50 which may be protected by gate oxide layer 48. Upon gate oxide layer 48 gate stacks 46 are disposed, each having spacers 44 made of a material preferably different in composition from dielectric 42. Besides spacer 44 being a silicon nitride, it may also be made from refractory metal nitrides such as cobalt nitride, titanium nitride, tungsten nitride, hafnium nitride, and the like.

In the first test, a self-aligned contact anisotropic etch is carried out as depicted in FIG. 3. In this example, spacer 44 is a nitride layer or a silicon dioxide layer that is doped differently from dielectric 42 and etching is carried out with CHF₃ under the inventive conditions. A contact 52 is formed in dielectric 42 and the first etching process using CHF₃ cuts into gate stack 46 by not being significantly selective to spacer 44 as it is exposed during the formation of contact 52. FIG. 3 illustrates damage to gate stack 46 due to the lack of selectivity to spacer 44 over dielectric 42 which is an oxide such as SiO₂, BPSG, TEOS, and PSG. Additionally, spacer 44 may be undoped oxide such as TEOS, or it may be an oxide with different doping from dielectric 42 including where dielectric 42 is undoped oxide.

In the test, semiconductive substrate 100 is etched using CHF₃ and CF₄ in a ratio of about 45 parts CHF₃ and 5 parts CF₄. Under equivalent etch conditions as those depicted in FIG. 3, FIG. 4 illustrates the formation of contact 52 down to the level of semiconductive material 50 where spacer 44 within contact 52 has been etched to a degree that is less than that depicted in FIG. 3, to form an eroded spacer 54. Where the etch conditions were similar to the first test, it is concluded that the presence of CF₄ has made the etch recipe more selective to the nitride of spacer 44 in order to form contact 52 and eroded spacer 54 to the degree where eroded spacer 54 may or may not be entirely laterally breached to expose electrically conductive elements such as polysilicon lines 58 within gate stack 46. Where it is preferable not to form eroded spacer 54, even where eroded spacer 54 is not entirely breached, it is instructive to conduct another example by increasing the amount of CF₄ gas in the etch recipe.

FIG. 5 illustrates a third test under the inventive conditions in which CF₄ has been increased to 15 parts in order to significantly increase selectivity to nitride. In other words, selectivity to spacer 44 during the formation of contact 52 has been enhanced to the point that spacer 44 disposed within contact 52 is substantially intact after the self-aligned anisotropic contact etch. Operating conditions for this example include CHF₃ in about 44 parts and CF₄ in about 13 to about 17 parts.

FIGS. 3-5 illustrate the enhanced selectivity to nitride of spacer 44 as a function of incrementally increasing the CF₄ gas. As thus illustrated in FIGS. 3-5, the degree of etch selectivity to spacer 44 is noted and the etch recipe may be adjusted until a preferred selectivity to spacer 44 has been determined.

Preferred processing conditions for the formation of contact 52 depicted in FIGS. 3-5, include power at outer antenna 32 in a range from about 700 watts to about 1,050 watts, preferably from about 775 watts to about 975 watts, and most preferably about 875 watts. Inner antenna 30 is operated under conditions in a range from about 100 watts to about 150 watts, preferably from about 115 watts to about 135 watts. Most preferably, when outer antenna 32 is operated at 875 watts, inner antenna 30 is operated at 125 watts. Bottom power applied to semiconductive substrate support 16 is operated in a range from about 500 watts to about 700 watts, preferably from about 550 watts to about 650 watts, and most preferably about 600 watts.

The temperature of semiconductive substrate support 16 is operated in a range from about −30° C. to about +80° C., preferably from about −20° C. to about +70° C., and most preferably about +40° C.

Performing Two Etches Within a Low Temperature Range

In another embodiment of the present invention, a combination of a mask-aligned, high-aspect ratio contact anisotropic etch and a self-aligned contact etch is carried out by using the inventive etch recipe and conditions. The inventive method proceeds by etching a contact under mask-aligned contact etch conditions that include a roof surface temperature in the etch chamber at or below about 200° C. Without changing the etch temperature range of the etch chamber, a second, high-aspect ratio etching of a self-aligned contact is carried out with CHF₃ and an etch selectivity fluorocarbon gas. The self-aligned contact etch is carried out at a roof surface temperature at or below about 190° C. in any of the above-mentioned preferred temperature ranges. This method of etching mask-aligned contacts and self-aligned contacts allows for the etch selectivity fluorocarbon gas to make the etch recipe more selective to the nitride layer. The above-mentioned ratios of etch selectivity fluorocarbon gases and proportions to the CHF₃ gases are also preferable for this embodiment. In particular, the etch selectivity fluorocarbon gas is preferably CF₄ and is supplied in a range from about 1 to about 15 parts and a hydrofluorocarbon gas, preferably CHF₃ is supplied in about 44 to about 45 parts.

In the present embodiment, the etch selectivity fluorocarbon gas preferably includes CF₄ as the only component, or as a major component in a range from about ¼ to about 9/1 of the etch selectivity fluorocarbon gas.

High-Aspect Ratio Etching

In another embodiment of the present invention, an etching method is provided for forming a high-aspect ratio contact in a semiconductive substrate. The method includes providing an IPS system 10 such as the Applied Materials IPS etch chamber. IPS system 10 has grounded silicon roof 14, semiconductive substrate supports 16, silicon ring 18, and other equipment as depicted in FIG. 1. Silicon roof 14 is operated at a roof surface temperature range from about 135° C. to about 190° C. Semiconductive substrate support 16 has a temperature range from about −30° C. to about +80° C., preferably from about −20° C. to about +70° C., and most preferably about +40° C. Silicon ring 18 is operated in a temperature range from about 180° C. to about 300° C., preferably from about 190° C. to about 250° C., and most preferably about 200° C.

The inventive method continues as illustrated in FIG. 6 by providing semiconductive substrate 200, having bulk dielectric 242 disposed upon an optional etch stop layer 248. Additionally, an etch stop layer may include semiconductive material 250, or any material that is compositionally different from bulk dielectric 242. Preferably bulk dielectric 242 is BPSG and etch stop layer 248 is a gate oxide, or generally silicon nitride, or Si₃N₄, or monocrystalline silicon with etch stop layer 248 optionally absent. Mask 240 overlies the bulk dielectric 242. The inventive method continues by anisotropiocally etching contact 252 as depicted in FIG. 6 with a hydrofluorocarbon such as CHF₃ etch gas and an etch selectivity fluorocarbon gas etch recipe, wherein the CHF₃ is flowed in a range from about 30 to about 50 sccm and the etch selectivity fluorocarbon gas is flowed in a range from about 1 to about 15 sccm.

Under the foregoing conditions, selectivity to etch stop layer 248 is increased as the proportion of fluorocarbon gas increases. Bulk dielectric 242 can be composed of BPSG, TEOS, and the like, and can also be a thermal silicon dioxide formed from either monocrystalline silicon or polycrystalline silicon. Etch stop layer 248 can be silicon nitride and may also be a thermally converted refractory metal nitride such as cobalt nitride, titanium nitride, tungsten nitride, hafnium nitride, and the like.

Etching with an Etch Selectivity Fluorocarbon Gas in an Etch System

In another embodiment in the present invention, a system of etching a semiconductive substrate is provided. The system includes an etcher such as an Applied Materials IPS chamber. IPS system 10 is operated under the temperature control conditions set forth herein for roof 14, semiconductive substrate support 16, and silicon ring 18. Other conditions include the above-mentioned flow rates, and pressures. The inventive system includes anisotropiocally etching the material of dielectric 42 in semiconductive substrate with a first etch recipe comprising CHF₃ and CF₄ in a first CF₄ proportion. Etching continues by etching the material of bulk dielectric 42 with a second etch recipe comprising CHF₃ in the same relative amount and CF₄ in a second, increased or decreased proportion, wherein etch selectivity is directly proportional to its increased amount or decreased amount of CF₄.

The present invention may be embodied in other specific forms without departing from its spirit or essential characteristics. The described embodiments are to be considered in all respects only as illustrative and not restrictive. The scope of the invention is, therefore, indicated by the appended claims rather than by the foregoing description. All changes which come within the meaning and range of equivalency of the claims are to be embraced within their scope. 

1. A method of removing silicon dioxide upon an etch stop layer, comprising: providing a silicon dioxide dielectric layer upon an etch stop layer, wherein the etch stop layer comprises silicon dioxide that is doped differently from the silicon dioxide dielectric layer; providing a gaseous etchant comprising a hydrofluorocarbon etch gas and a fluorocarbon selectivity compound; and exposing the silicon dioxide dielectric layer to the gaseous etchant.
 2. The method of claim 1, wherein the fluorocarbon selectivity compound is selected from the group consisting of CF₄, C₂F₆, C₄F₈, C₅F₆, C₅F₈, and combinations thereof.
 3. The method of claim 1, wherein the hydrofluorocarbon etch gas is provided in a first quantity, the fluorocarbon selectivity compound is provided in a second quantity, and the first quantity is at least twice the second quantity.
 4. The method of claim 1, further comprising etching the silicon dioxide dielectric layer in the gaseous etchant until the etch stop layer is exposed.
 5. The method of claim 1, wherein providing a gaseous etchant further comprises providing a gaseous etchant comprising about 30 parts to about 50 parts of a hydrofluorocarbon etch gas comprising CHF₃ and about less than one part to about 15 parts of a fluorocarbon selectivity compound.
 6. The method of claim 1, wherein providing a gaseous etchant further comprises providing a gaseous etchant comprising about 44 parts to about 45 parts of a hydrofluorocarbon etch gas comprising CHF₃ and about 0.5 parts to about 4 parts of a fluorocarbon selectivity compound.
 7. A method of removing silicon dioxide upon an etch stop layer, comprising: providing a silicon dioxide dielectric layer upon an etch stop layer, wherein the etch stop layer comprises silicon dioxide that is doped differently from the silicon dioxide dielectric layer; providing a first gaseous etchant comprising a hydrofluorocarbon etch gas; providing a second gaseous etchant comprising a fluorocarbon selectivity compound; and exposing the silicon dioxide dielectric layer to the first gaseous etchant and the second gaseous etchant.
 8. The method of claim 7, wherein the fluorocarbon selectivity compound of the second gaseous etchant is selected from the group consisting of CF₄, C₂F₆, C₄F₈, C₅F₆, C₅F₈, and combinations thereof.
 9. The method of claim 7, wherein the first gaseous etchant is provided in a first quantity, the second gaseous etchant is provided in a second quantity, and the first quantity is at least twice the second quantity.
 10. The method of claim 7, further comprising etching the silicon dioxide dielectric layer in a mixture of the first gaseous etchant and the second gaseous etchant.
 11. The method of claim 7, wherein exposing the silicon dioxide dielectric layer to the first gaseous etchant and the second gaseous etchant comprises exposing the silicon dioxide dielectric layer to the first gaseous etchant and the second gaseous etchant simultaneously.
 12. The method of claim 7, wherein: providing a first gaseous etchant further comprises providing a first gaseous etchant comprising about 30 parts to about 50 parts of a hydrofluorocarbon etch gas comprising CHF₃; and wherein providing a second gaseous etchant further comprises providing a second gaseous etchant comprising about less than one part to about 15 parts of a fluorocarbon selectivity compound.
 13. The method of claim 7, wherein: providing a first gaseous etchant further comprises providing a first gaseous etchant comprising about 44 parts to about 45 parts of a hydrofluorocarbon etch gas comprising CHF₃; and wherein providing a second gaseous etchant further comprises providing a second gaseous etchant comprising about 0.5 parts to about 4 parts of a fluorocarbon selectivity compound.
 14. The method of claim 7, wherein exposing the silicon dioxide dielectric layer to the first gaseous etchant and the second gaseous etchant further comprises: exposing the silicon dioxide dielectric layer to a constant supply of the first gaseous etchant; and intermittently exposing the silicon dioxide dielectric layer to the second gaseous etchant wherein the second gaseous etchant is intermittently blended with the first gaseous etchant.
 15. A method of removing silicon dioxide upon an etch stop layer, comprising: providing a silicon dioxide dielectric layer upon an etch stop layer, wherein the etch stop layer comprises silicon dioxide that is doped differently from the silicon dioxide dielectric layer; providing a first gaseous etchant comprising a hydrofluorocarbon etch gas; providing a second gaseous etchant comprising a fluorocarbon selectivity compound; exposing the silicon dioxide dielectric layer to the first gaseous etchant; and pulsing the second gaseous etchant into the first gaseous etchant during the exposing of the silicon dioxide dielectric layer to the first gaseous etchant to expose the silicon dioxide dielectric layer to a mixture of the first gaseous etchant and the second gaseous etchant.
 16. The method of claim 15, wherein the fluorocarbon selectivity compound of the second gaseous etchant is selected from the group consisting of CF₄, C₂F₆, C₄F₈, C₅F₆, C₅F₈, and combinations thereof.
 17. The method of claim 15, wherein the first gaseous etchant is provided in a first quantity, the second gaseous etchant is provided in a second quantity, and the first quantity is at least twice the second quantity.
 18. The method of claim 15, further comprising etching the silicon dioxide dielectric layer in a mixture of the first gaseous etchant and the second gaseous etchant until the etch stop layer is exposed.
 19. The method of claim 15, wherein providing a first gaseous etchant further comprises providing a first gaseous etchant comprising about 30 parts to about 50 parts of a hydrofluorocarbon etch gas comprising CHF₃.
 20. The method of claim 15, wherein providing a first gaseous etchant further comprises providing a first gaseous etchant comprising about 44 parts to about 45 parts of a hydrofluorocarbon etch gas comprising CHF₃.
 21. The method of claim 15, wherein providing a second gaseous etchant further comprises providing a second gaseous etchant comprising about less than one part to about 15 parts of a fluorocarbon selectivity compound.
 22. The method of claim 15, wherein providing a second gaseous etchant further comprises providing a second gaseous etchant comprising about 0.5 parts to about 4 parts of a fluorocarbon selectivity compound. 